The Recall Desk
SevereFDA (Devices)·Z-1850-2017·Announced 2017-04-26

Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment

Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II and involves a structural defect (blade detachment/fracture) in a surgical instrument, which poses a significant risk of injury during a procedure.

Plain-English summary

Smith & Nephew, Inc. is recalling the ACUFEX TRUNAV Retrograde Drill 11.5MM (Product Number: 72204049). The device is intended for use in creating a back bore socket in bone. The recall involves batch numbers G11227 and G18820.

The recall was initiated due to a potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming. This is classified as an FDA Class II recall.

The affected products were distributed worldwide, including nationwide in the US and internationally to Australia, Chile, Denmark, Germany, Spain, France, Great Britain, the Netherlands, and Sweden. Healthcare providers should stop using the affected devices and contact Smith & Nephew for further instructions.

The recalled product

Product
Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11.5MM Product Number: 72204049 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
Manufacturer
Smith & Nephew, Inc.
Category
Medical Device — Surgical Instrument
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Batch Numbers: G11227
  • G18820

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 14 recalled by Smith & Nephew, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 14 products in this recall →

Related recalls

Same manufacturer · Smith & Nephew, Inc.

See all →

Same hazard · blade detachment

See all →